Senior Engineer

• Actively shape the process development and ensuring that all activities are completed and documented in accordance with the Stryker procedures.
• Coordinate with internal and external partners, responsible for solving technical challenges and implementing efficient manufacturing and testing strategies in a highly technical environment.
• Make a significant contribution to the realization of short transfer times, considering innovative problem-solving methods, continuous development and optimization of our manufacturing processes.
• Work closely with cross functional teams and international project teams and process experts.
• Participate in PFMEA, Control Plan, SOP and PPAP generation associated with product transfers. 
• Complete capability and MSA studies for in process inspection and generate subsequent Inspection documentation.

What will you need

Basic Qualifications:

• Master's or bachelor's degree in engineering (automation technology, process engineering, electrical engineering, mechanical engineering, medical technology, industrial engineering or similar) with 5 to 8 years of professional experience in the field of process development and/or process optimization.
• Hands on experience with Medical Device Post Market Surveillance.
• Experience with Product development/ Transfer, Process Engineering, Supplier development /PPAP.
• Good knowledge of manufacturing processes, materials, product and process design. 
• Able to read and interpret complex engineering drawings and has the ability to understand geometrical dimensioning and tolerancing. 

Preferred Qualifications:

• Excellent Interpersonal and analytical Skills.
• Individual is willing to travel occasionally for business purposes
• Experience in an FDA regulated or regulated industry beneficial